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Stress During Deep Sedation With Propofol With and Without Alfentanil

Sedation Clinical Trial

Official title:
Physiologic Stress During Procedural Sedation With and Without Alfentanil

Clinical Trial Summary

This is a randomized clinical trial of deep procedural sedation with propofol with and without supplemental alfentanil. Patients will be assessed for total and fractionated serum catecholamines before and after the procedure in addition to usual procedural sedation outcomes parameters to assess the adrenergic effect of propofol sedation without supplemental opioid.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00997113
Study type Interventional
Source Minneapolis Medical Research Foundation
Contact
Status Completed
Phase Phase 4
Start date October 2009
Completion date December 2012
View Details
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